Discovery of the First-in-Class Dual-Target ROCK/HDAC Inhibitor with Potent Antitumor Efficacy in Vivo That Trigger Antitumor Immunity

Triple-negative breast cancer (TNBC) represents a highly aggressive and heterogeneous malignancy. Currently, multitarget drug approaches present a promising therapeutic approach for TNBC. Utilizing a combinatorial chemistry strategy to construct a virtual screening database, dual ROCK/HDAC-targeting benzothiophene compounds were identified. Notably, compound <b>10h</b> effectively inhibits ROCK1/2 and HDAC1/2/3/6/8 while demonstrating potent antiproliferative activity against breast cancer cells. In an orthotopic mouse model of breast cancer, <b>10h</b> significantly suppressed tumor growth without apparent toxicity. Importantly, <b>10h</b> induced immunogenic cell death (ICD), promoted dendritic cells (DCs) maturation, and activated T cells, thereby initiating antitumor immunity. In conclusion, compound <b>10h</b> is a novel dual-target ROCK/HDAC inhibitor that represents a promising treatment strategy for TNBC.

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Publication Details

Journal
Journal of Medicinal Chemistry
Published
2024-11-11
DOI
https://doi.org/10.1021/acs.jmedchem.4c02183
Citations
14
Primary Topic
Histone Deacetylase Inhibitors Research
Type
article
Field-Weighted Citation Impact
3.27

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article

Discovery of the First-in-Class Dual-Target ROCK/HDAC Inhibitor with Potent Antitumor Efficacy in Vivo That Trigger Antitumor Immunity

Jiebin Fang, Ningjing Zhang, Yun Yan Huang, Shijie Zou et al.
14 citations
Journal of Medicinal Chemistry
Histone Deacetylase Inhibitors Research
3.27
article

Discovery of the First-in-Class Dual-Target ROCK/HDAC Inhibitor with Potent Antitumor Efficacy in Vivo That Trigger Antitumor Immunity

Jiebin Fang, Ningjing Zhang, Yun Yan Huang, Shijie Zou, Wanjing Ding, Zhongjun Ma, Zhenghan Fang, Xiaohong Chen, Zhe Chen, Churu Mao, Xia Ding, Yijie Lou
article en
14 citations

Abstract

Triple-negative breast cancer (TNBC) represents a highly aggressive and heterogeneous malignancy. Currently, multitarget drug approaches present a promising therapeutic approach for TNBC. Utilizing a combinatorial chemistry strategy to construct a virtual screening database, dual ROCK/HDAC-targeting benzothiophene compounds were identified. Notably, compound <b>10h</b> effectively inhibits ROCK1/2 and HDAC1/2/3/6/8 while demonstrating potent antiproliferative activity against breast cancer cells. In an orthotopic mouse model of breast cancer, <b>10h</b> significantly suppressed tumor growth without apparent toxicity. Importantly, <b>10h</b> induced immunogenic cell death (ICD), promoted dendritic cells (DCs) maturation, and activated T cells, thereby initiating antitumor immunity. In conclusion, compound <b>10h</b> is a novel dual-target ROCK/HDAC inhibitor that represents a promising treatment strategy for TNBC.

Journal of Medicinal ChemistryVol. 67(22)
Zhejiang Chinese Medical University (CN), Zhejiang Ocean University (CN), Sanya University (CN), Zhejiang University (CN)
National Natural Science Foundation of China
Zero hunger
Openalex Percentile: Top 7%
Histone Deacetylase Inhibitors Research
3.27
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